Package 63323-599-30

Brand: deferoxamine

Generic: deferoxamine mesylate
NDC Package

Package Facts

Identity

Package NDC 63323-599-30
Digits Only 6332359930
Product NDC 63323-599
Product ID 63323-599_6e384a23-a8c4-455a-b84b-847393d491e6
Description

1 VIAL in 1 BOX (63323-599-30) / 21.1 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2009-12-15
Brand deferoxamine
Generic deferoxamine mesylate
Sample Package No

Linked Drug Pages (1)

Deferoxamine ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "6e384a23-a8c4-455a-b84b-847393d491e6", "openfda": {"upc": ["0363323599300", "0363323597108"], "unii": ["V9TKO7EO6K"], "rxcui": ["1731345", "1731350"], "spl_set_id": ["d91e16df-8daa-4cd2-86a2-273eaa2446e0"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (63323-599-30)  / 21.1 mL in 1 VIAL", "package_ndc": "63323-599-30", "marketing_start_date": "20091215"}], "brand_name": "Deferoxamine", "product_id": "63323-599_6e384a23-a8c4-455a-b84b-847393d491e6", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Iron Chelating Activity [MoA]", "Iron Chelator [EPC]"], "product_ndc": "63323-599", "generic_name": "DEFEROXAMINE MESYLATE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Deferoxamine", "active_ingredients": [{"name": "DEFEROXAMINE MESYLATE", "strength": "95 mg/mL"}], "application_number": "ANDA078718", "marketing_category": "ANDA", "marketing_start_date": "20091215", "listing_expiration_date": "20261231"}